2 research outputs found
Fabrication of 3D Macroscopic Graphene Oxide Composites Supported by Montmorillonite for Efficient U(VI) Wastewater Purification
In this work, montmorillonite (MMT)
was intercalated into a sheet
of GO and then cross-linked by agar, realizing the 3D macroscopic
composites of agar-MMT-GO. Agar-MMT-GO composites were characterized
by SEM, TEM, FTIR, TGA, and XPS techniques. Fabricated agar-MMT-GO
composites were tough and lightweight materials with a multichannel
structure. The heat stability of agar-MMT-GO composites were enhanced
relative to GO, as demonstrated by TGA results. FTIR analysis testified
to no chemical bond between GO and MMT component, suggesting that
agar scaffold mainly caused the formation of agar-MMT-GO composites.
Agar-MMT-GO composites exhibited a good performance in UÂ(VI) sorption
(<i>Q</i><sub>max</sub> of 147 mg/g at pH 4.5) and in recycling
tests. The rate-limiting sorption step was the diffusion of UÂ(VI)
from liquid solution to the surface sites of agar-MMT-GO composites.
XPS analysis demonstrated that UÂ(VI) sorption on agar-MMT-GO was mainly
attributed to cation exchange and inner-sphere complexation in low
and high pH regions, respectively. Briefly, our work here provides
new insights in designing GO composites with a solid skeleton to promote
its large-scale application in wastewater remediation
Microscopic and Spectroscopic Insights into Uranium Phosphate Mineral Precipitated by <i>Bacillus Mucilaginosus</i>
In this paper, we used spectroscopic
and microscopic techniques to investigate the interaction mechanism
between uranium and <i>Bacillus mucilaginosus</i>. According
to scanning electron microscope couple with energy dispersive X-ray
detector analysis, the lamellar uranium phosphate precipitation was
only observed on the living <i>B. mucilaginosus</i> and
the resting <i>B. mucilaginosus</i>. The Fourier transform
infrared spectroscopy spectrum also indicated the important role of
phosphate groups in forming UÂ(VI)-phosphates precipitation. The X-ray
diffraction analysis identified the phase of UÂ(VI)-phosphate precipitation
as H<sub>3</sub>OUO<sub>2</sub>PO<sub>4</sub>·3H<sub>2</sub>O.
Batch experiment showed that biominerilization amount could be up
to 195.84 mg/g when exposing living <i>B. mucilaginosus</i> to UÂ(VI) aqueous solution at pH 5.0 for 1 h. The precipitate was
further evidenced by extended X-ray absorption fine structure spectra
based on the presence of U–P shell, which demonstrated that
hydrogen uranyl phosphate became the main products on the living <i>B. mucilaginosus</i> with prolonged reacting time. After ashing
and hydrothermal process, the precipitated UÂ(VI) on <i>B. mucilaginosus</i> could be converted into UO<sub>2</sub> and KÂ(UO<sub>2</sub>)Â(PO<sub>4</sub>)·3H<sub>2</sub>O. Our findings have significant implications
in elucidating the potential role of bacteria in the migration of
uranium in geological environment